document record

Cilag AG in Schaffhausen, part of Johnson & Johnson, is hiring for an Operator (m/f/d) in sterile pharmaceutical manufacturing. You will operate state-of-the-art equipment, ensure GMP compliance and document activities. The role supports process improvements, batch records, cleaning and maintenance, and works within a 3-shift schedule.German language skills...

Johnson & Johnson in Schaffhausen is seeking a Manufacturing Operator - Compounding to operate and monitor modern sterile pharmaceutical production equipment under GMP conditions, ensuring safe, high‑quality medicines and timely output. You will perform GMP-relevant tasks, document batch records and logbooks, assist with process improvements, and work in a...

Job DescriptionJob Title:Word and PDF ExpertsJob Type:ContractLocation:RemoteJob Summary:In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.Key...

pWe are looking for an experienced bGMP Officer (QC) /b to support Quality Control activities within a pharmaceutical environment. The role is focused on bGMP compliance, investigations, deviations, CAPAs and quality documentation /b, working closely with both QC and QA teams. /ph3Job Duties /h3ulliAuthor and manage deviations, investigations and change...

pbThis position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Quality Systems Manager based in Switzerland. /b /ppThis is a corporate-level quality leadership role focused on maintaining and continuously improving a standardized Quality Management System across multiple facilities....

pJoin our client and play a key role in maintaining top-tier quality standards! If you have a keen eye for detail and a passion for compliance, this could be your perfect opportunity. /p pProclinical is seeking a QA Associate III to join the Integrated Downstream Quality Operations team at a large-scale manufacturing facility. In this role, you will focus on...

QA Specialist – 7079Our client, a global pharmaceutical company, is looking for a QA Specialist to support Quality Assurance activities related to Investigational Medicinal Products (IMPs).The role focuses on GMP documentation review, quality system activities, batch documentation, and coordination with Contract Manufacturing Organizations (CMOs). The...

QA Specialist – 7079Our client, a global pharmaceutical company, is looking for a QA Specialist to support Quality Assurance activities related to Investigational Medicinal Products (IMPs).The role focuses on GMP documentation review, quality system activities, batch documentation, and coordination with Contract Manufacturing Organizations (CMOs). The...

Job DescriptionJob Title: Word and PDF ExpertsJob Type: ContractLocation: RemoteJob Summary: In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.Key...

Fluent Language Skills Required: Gujarati. Native fluency in Gujarati, including full command of Gujarati script and orthography, is required for this position. All annotation and transcription work is performed in Gujarati. Why This Role Exists Document understanding breaks down fastest in the languages that parsing and vision-language models rarely see....

Fluent Language Skills Required: Japanese. Native fluency in Japanese, including full command of kanji, hiragana and katakana, is required for this position. All annotation and transcription work is performed in Japanese. Why This Role Exists Document understanding breaks down fastest in the languages that parsing and vision-language models rarely see. This...

Fluent Language Skills Required: Bengali. Native fluency in Bengali, including full command of Bengali script and orthography, is required for this position. All annotation and transcription work is performed in Bengali. Why This Role Exists Document understanding breaks down fastest in the languages that parsing and vision-language models rarely see. This...

pFor one of our clients, a financial institution based in Geneva, we are looking for a: /p h3CENTRAL FILE OFFICER /h3 ul liCoding the client data in the IT systems: entry and configuration the account openings, /li liPerform due diligence on customers, using methods such as data analysis and document verification /li liPrepare and manage reports on customer...

W Hotels Verbier is seeking an Administrative professional to join our team at Rue de Medran 70, Verbier, Switzerland. This full-time, non-management role focuses on data entry, records maintenance, and guest support while upholding Marriott's service standards.Responsibilities include processing information, preparing documents, and ensuring confidentiality...

h3Technical Author /h3 pBachem SA Vacant since : Number of jobs : 1 1895 Vionnaz (VS) 100% Immediately Permanent /p pBachem is a world leader in the development and manufacture of peptides and oligonucleotides for thepharmaceutical industry. To strengthen our Technical Operations team in Vionnaz (Valais, Switzerland), we arelooking for aTechnical Author...

Florence Unified School District is seeking an Auction & Procurement Processor to coordinate surplus property and the district's auction process. You will identify, document, remove from inventory, list for auction, and transfer surplus items to purchasers per district policies and state regulations.You will handle online auction site management, asset...

pVous résidez dans la région du Locle, de Neuchâtel ou en zone frontalière ? Vous disposez d'une expérience en Système Qualité avec une appétence pour la gestion documentaire (Record Management) dans l'industrie médicale ou technique ? /ppPour le compte d'un acteur majeur de l'industrie médicale basé au Locle, nous recherchons un(e) : /ph3Lieu...

ten23 health is seeking Visual Inspection Operators to join our Visp site as a crucial step in quality control. You will perform manual visual inspections of vials, syringes, and cartridges and document results in GMP-compliant records.We provide internal training, flexible working arrangements, and a culture that values openness and collaboration. German...

ph3Senior Business Analyst / Requirements Engineer /h3h3About the job Senior Business Analyst / Requirements Engineer /h3pbPrimary Responsibilities: /b /ppCollaborate with business units to identify and define requirements /ppAnalyze current processes and support the development of potential solutions /ppPlan, lead, and document workshops and...

ph3SOMMAIRE /h3 pLe senior technicien de production exerce un rôle opérationnel en pilotant les outils de production en accord avec les règles GMP. /p h3Aperçu /h3 pLe senior technicien de production exerce un rôle opérationnel en pilotant les outils de production en accord avec les règles GMP. Le département DSP est responsable de la purification...